Literature DB >> 22884960

Cortisol and inflammatory processes in ovarian cancer patients following primary treatment: relationships with depression, fatigue, and disability.

Andrew Schrepf1, Lauren Clevenger, Desire Christensen, Koen DeGeest, David Bender, Amina Ahmed, Michael J Goodheart, Laila Dahmoush, Frank Penedo, Joseph A Lucci, Parvin Ganjei-Azar, Luis Mendez, Kristian Markon, David M Lubaroff, Premal H Thaker, George M Slavich, Anil K Sood, Susan K Lutgendorf.   

Abstract

Elevations in the pro-inflammatory cytokine interleukin-6 (IL-6) and alterations in the anti-inflammatory hormone cortisol have been reported in a variety of cancers. IL-6 has prognostic significance in ovarian cancer and cortisol has been associated with fatigue, disability, and vegetative depression in ovarian cancer patients prior to surgery. Ovarian cancer patients undergoing primary treatment completed psychological self-report measures and collected salivary cortisol and plasma IL-6 prior to surgery, at 6 months, and at 1 year. Patients included in this study had completed chemotherapy and had no evidence of disease recurrence. At 6 months, patients showed significant reductions in nocturnal cortisol secretion, plasma IL-6, and a more normalized diurnal cortisol rhythm, changes that were maintained at 1 year. The reductions in IL-6 and nocturnal cortisol were associated with declines in self-reported fatigue, vegetative depression, and disability. These findings suggest that primary treatment for ovarian cancer reduces the inflammatory response. Moreover, patients who have not developed recurrent disease by 1 year appear to maintain more normalized levels of cortisol and IL-6. Improvement in fatigue and vegetative depression is associated with the normalization of IL-6 and cortisol, a pattern which may be relevant for improvements in overall quality of life for ovarian cancer patients.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22884960      PMCID: PMC3697797          DOI: 10.1016/j.bbi.2012.07.022

Source DB:  PubMed          Journal:  Brain Behav Immun        ISSN: 0889-1591            Impact factor:   7.217


  79 in total

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